Variant report

Variant	nsv1001906
Chromosome Location	chr4:55447189-55505721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:220)
CpG islands
(count:184)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:220 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:55452430-55452826	K562	blood:	n/a	n/a
2	ARID3A	chr4:55454394-55455108	K562	blood:	n/a	n/a
3	ARID3A	chr4:55451642-55452190	K562	blood:	n/a	n/a
4	ATF1	chr4:55451820-55452249	K562	blood:	n/a	n/a
5	ATF3	chr4:55451714-55452065	K562	blood:	n/a	n/a
6	BHLHE40	chr4:55454595-55455217	K562	blood:	n/a	n/a
7	BHLHE40	chr4:55451901-55452642	K562	blood:	n/a	n/a
8	BHLHE40	chr4:55481802-55481953	K562	blood:	n/a	n/a
9	BHLHE40	chr4:55452884-55453067	K562	blood:	n/a	n/a
10	CCNT2	chr4:55451641-55452101	K562	blood:	n/a	n/a
11	CCNT2	chr4:55454457-55454926	K562	blood:	n/a	chr4:55454690-55454710
12	CEBPB	chr4:55480281-55480639	H1-hESC	embryonic stem cell:	n/a	chr4:55480456-55480467
13	CEBPB	chr4:55480277-55480651	IMR90	lung:	n/a	chr4:55480456-55480467
14	CEBPB	chr4:55486081-55486233	K562	blood:	n/a	n/a
15	CEBPB	chr4:55463042-55463257	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:55480297-55480591	A549	lung:	n/a	chr4:55480456-55480467
17	CEBPB	chr4:55487007-55487179	K562	blood:	n/a	n/a
18	CEBPB	chr4:55487969-55488142	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:55480250-55480626	MCF-7	breast:	n/a	chr4:55480456-55480467
20	CEBPB	chr4:55480285-55480648	HepG2	liver:	n/a	chr4:55480456-55480467
21	CEBPB	chr4:55480387-55480632	Hela-S3	cervix:	n/a	chr4:55480456-55480467
22	CEBPB	chr4:55491744-55491864	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:55487970-55488194	K562	blood:	n/a	n/a
24	CEBPB	chr4:55452578-55452765	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:55480337-55480621	ECC-1	luminal epithelium:	n/a	chr4:55480456-55480467
26	CEBPB	chr4:55480277-55480655	K562	blood:	n/a	chr4:55480456-55480467
27	CEBPB	chr4:55487953-55488193	K562	blood:	n/a	n/a
28	CEBPB	chr4:55480323-55480618	K562	blood:	n/a	chr4:55480456-55480467
29	CEBPB	chr4:55480285-55480623	ECC-1	luminal epithelium:	n/a	chr4:55480456-55480467
30	CEBPB	chr4:55480333-55480704	MCF-7	breast:	n/a	chr4:55480456-55480467
31	CEBPD	chr4:55454456-55454975	K562	blood:	n/a	n/a
32	CEBPD	chr4:55454429-55454953	K562	blood:	n/a	n/a
33	CHD2	chr4:55451564-55451677	K562	blood:	n/a	n/a
34	CTCF	chr4:55471180-55471330	HepG2	liver:	n/a	n/a
35	CTCF	chr4:55499067-55499171	K562	blood:	n/a	n/a
36	CTCF	chr4:55499046-55499190	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr4:55468616-55468686	GM10248	blood:	n/a	n/a
38	CTCF	chr4:55449076-55449112	Lung_OC	lung:	n/a	n/a
39	CTCF	chr4:55471147-55471348	K562	blood:	n/a	n/a
40	CTCF	chr4:55471180-55471330	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr4:55471140-55471290	HAc	cerebellar:	n/a	n/a
42	CTCF	chr4:55470107-55470224	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr4:55489050-55489087	Lung_OC	lung:	n/a	n/a
44	CTCF	chr4:55451707-55452048	K562	blood:	n/a	n/a
45	CTCF	chr4:55453700-55453850	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr4:55471246-55471344	K562	blood:	n/a	n/a
47	CTCF	chr4:55471256-55471332	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:55471320-55471470	HRPEpiC	eye:	n/a	n/a
49	CUX1	chr4:55452950-55453042	K562	blood:	n/a	n/a
50	CUX1	chr4:55481835-55482035	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:55499029-55499079	AoSMC	blood vessel:	n/a
2	chr4:55499029-55499079	AoSMC	blood vessel:	n/a
3	chr4:55499684-55499734	AG04450	lung:	fetal
4	chr4:55499029-55499079	NB4	blood:	n/a
5	chr4:55499384-55499434	HCM	heart:	n/a
6	chr4:55499029-55499079	SKMC	muscle:	n/a
7	chr4:55499684-55499734	NB4	blood:	n/a
8	chr4:55499684-55499734	NT2-D1	testis:	n/a
9	chr4:55499684-55499734	PANC-1	pancreas:	n/a
10	chr4:55499684-55499734	Hepatocyte	liver:	n/a
11	chr4:55499029-55499079	MCF10A-Er-Src	breast:	n/a
12	chr4:55499684-55499734	AG10803	skin:	n/a
13	chr4:55499384-55499434	NHDF-neo	bronchial:	n/a
14	chr4:55499384-55499434	HMEC	breast:	n/a
15	chr4:55499384-55499434	GM12892	blood:	n/a
16	chr4:55499684-55499734	GM06990	blood:	n/a
17	chr4:55499384-55499434	HRPEpiC	eye:	n/a
18	chr4:55499684-55499734	Caco-2	colon:	n/a
19	chr4:55499029-55499079	HEK293	kidney:	embryo
20	chr4:55499029-55499079	GM19239	blood:	n/a
21	chr4:55499029-55499079	Hela-S3	cervix:	n/a
22	chr4:55499684-55499734	A549	lung:	n/a
23	chr4:55499029-55499079	PANC-1	pancreas:	n/a
24	chr4:55499384-55499434	SKMC	muscle:	n/a
25	chr4:55499684-55499734	U87	brain:	n/a
26	chr4:55499384-55499434	T-47D	breast:	n/a
27	chr4:55499384-55499434	GM12891	blood:	n/a
28	chr4:55499384-55499434	SAEC	small airway:	n/a
29	chr4:55499384-55499434	A549	lung:	n/a
30	chr4:55499684-55499734	SAEC	small airway:	n/a
31	chr4:55499684-55499734	HRPEpiC	eye:	n/a
32	chr4:55499029-55499079	CMK	blood:	n/a
33	chr4:55499384-55499434	HRCEpiC	kidney:	n/a
34	chr4:55499384-55499434	SK-N-SH_RA	brain:	n/a
35	chr4:55499029-55499079	HepG2	liver:	n/a
36	chr4:55499684-55499734	AG09319	gingival:	n/a
37	chr4:55499029-55499079	ovcar-3	ovarian:	n/a
38	chr4:55499684-55499734	IMR90	lung:	fetal
39	chr4:55499684-55499734	NHBE	bronchial:	n/a
40	chr4:55499029-55499079	RPTEC	kidney:	n/a
41	chr4:55499029-55499079	HNPCEpiC	eye:	n/a
42	chr4:55499029-55499079	A549	lung:	n/a
43	chr4:55499384-55499434	AG10803	skin:	n/a
44	chr4:55499384-55499434	AG09319	gingival:	n/a
45	chr4:55499384-55499434	HCPEpiC	choroid plexus:	n/a
46	chr4:55499384-55499434	HIPEpiC	eye:	n/a
47	chr4:55499029-55499079	HCT-116	colon:	n/a
48	chr4:55499029-55499079	SAEC	small airway:	n/a
49	chr4:55499384-55499434	HL-60	blood:	n/a
50	chr4:55499029-55499079	BE2_C	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:55444047..55449090-chr4:55449528..55453666,5	K562	blood:
2	chr4:55445449..55448428-chr4:55450519..55452386,2	K562	blood:
3	chr4:55500450..55502781-chr4:55503910..55506040,3	K562	blood:
4	chr4:55445449..55448428-chr4:55450519..55452386,2	K562	blood:
5	chr4:55444047..55449090-chr4:55449528..55453666,5	K562	blood:
6	chr4:55437669..55439693-chr4:55458499..55461313,2	K562	blood:
7	chr4:55454057..55456596-chr4:55458841..55461034,2	K562	blood:
8	chr4:55500450..55502781-chr4:55503910..55506040,3	K562	blood:
9	chr4:55455740..55458184-chr4:55518555..55520404,2	K562	blood:
10	chr4:55453068..55455873-chr4:55797216..55798753,2	MCF-7	breast:
11	chr4:55502404..55505387-chr4:55506992..55509953,2	MCF-7	breast:
12	chr4:55452869..55453638-chr4:55708509..55709111,2	MCF-7	breast:
13	chr4:55503201..55504980-chr4:55510390..55512353,2	K562	blood:
14	chr4:55481868..55484293-chr4:55528991..55530564,2	K562	blood:
15	chr20:52457233..52457942-chr4:55449043..55449853,2	MCF-7	breast:
16	chr4:55451154..55453615-chr4:55461278..55463785,2	MCF-7	breast:
17	chr4:55454057..55456596-chr4:55458841..55461034,2	K562	blood:
18	chr4:55459508..55460256-chr4:55524686..55525285,2	MCF-7	breast:
19	chr4:55436094..55437601-chr4:55449957..55451605,2	K562	blood:
20	chr4:55451154..55453615-chr4:55461278..55463785,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDR-2	chr4:55469380-55471344	XLOC_003949
2	lnc-KDR-2	chr4:55473050-55473298	XLOC_003949
3	lnc-KDR-2	chr4:55469378-55471344	ENSG00000250456
4	lnc-KDR-2	chr4:55473050-55473298	ENSG00000250456

No data

Variant related genes	Relation type
ENSG00000250456	TF binding region
ENSG00000250456	CpG island
LITAF	miRNA target sites

Extended variants
information (count: 1638 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1638 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142963478	chr4:55447223-55447224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182581509	chr4:55447250-55447251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs151045267	chr4:55447258-55447259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187552922	chr4:55447259-55447260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190563894	chr4:55447295-55447296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549631763	chr4:55447296-55447297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2703468	chr4:55447311-55447312	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs528642369	chr4:55447333-55447334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140930498	chr4:55447336-55447337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146655428	chr4:55447455-55447456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536996244	chr4:55447471-55447472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550068391	chr4:55447481-55447482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139093692	chr4:55447485-55447486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535720631	chr4:55447488-55447489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2537875	chr4:55447500-55447501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs557498547	chr4:55447531-55447532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571902357	chr4:55447596-55447597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575937378	chr4:55447636-55447637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543275299	chr4:55447689-55447690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561827954	chr4:55447691-55447692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374998844	chr4:55447692-55447693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556901337	chr4:55447697-55447698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368845682	chr4:55447707-55447708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574279132	chr4:55447738-55447739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574824070	chr4:55447755-55447756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543339107	chr4:55447830-55447831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560028168	chr4:55447838-55447839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141344137	chr4:55447840-55447841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545519531	chr4:55447841-55447842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6817676	chr4:55447888-55447889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs372553938	chr4:55447911-55447912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138099866	chr4:55447977-55447978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567650889	chr4:55448022-55448023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368618429	chr4:55448023-55448024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111655200	chr4:55448027-55448028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201562765	chr4:55448037-55448038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs202236856	chr4:55448038-55448039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs28649356	chr4:55448039-55448040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs149544410	chr4:55448043-55448044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111804839	chr4:55448052-55448053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192478893	chr4:55448054-55448055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144130244	chr4:55448076-55448077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2703469	chr4:55448100-55448101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs80029796	chr4:55448128-55448129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184508639	chr4:55448138-55448139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs56018625	chr4:55448148-55448149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115053140	chr4:55448159-55448160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186468779	chr4:55448162-55448163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531931494	chr4:55448169-55448170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113553103	chr4:55448210-55448211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164920	CNVD
Cancer	22183965	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55441600-55450600	Weak transcription	K562	blood
2	chr4:55448400-55449200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:55449200-55452000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:55450600-55451400	Enhancers	K562	blood
5	chr4:55451400-55452200	Enhancers	Duodenum Mucosa	Duodenum
6	chr4:55451400-55452200	Flanking Active TSS	K562	blood
7	chr4:55451400-55453200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:55451400-55453800	Enhancers	Fetal Intestine Large	intestine
9	chr4:55451400-55454000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:55451800-55452400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:55451800-55452600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr4:55451800-55453200	Enhancers	NHDF-Ad	bronchial
13	chr4:55452000-55452600	Enhancers	Osteobl	bone
14	chr4:55452000-55453000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:55452000-55453000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr4:55452000-55453600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:55452000-55453800	Enhancers	Fetal Intestine Small	intestine
18	chr4:55452000-55453800	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr4:55452000-55454000	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr4:55452000-55455400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:55452000-55455400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:55452000-55455800	Enhancers	HMEC	breast
23	chr4:55452000-55457200	Enhancers	NHEK	skin
24	chr4:55452000-55457600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:55452200-55452600	Flanking Active TSS	Duodenum Mucosa	Duodenum
26	chr4:55452200-55453000	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr4:55452200-55453200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr4:55452200-55455400	Enhancers	K562	blood
29	chr4:55452400-55452800	Enhancers	NH-A	brain
30	chr4:55452400-55453000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:55452400-55453000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr4:55452400-55453000	Enhancers	Lung	lung
33	chr4:55452400-55453000	Enhancers	NHLF	lung
34	chr4:55452400-55453800	Enhancers	Esophagus	oesophagus
35	chr4:55452400-55453800	Enhancers	Placenta	Placenta
36	chr4:55452400-55454000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:55452600-55453800	Enhancers	Duodenum Mucosa	Duodenum
38	chr4:55453000-55453400	Enhancers	Stomach Mucosa	stomach
39	chr4:55453200-55454400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr4:55453400-55454400	Weak transcription	Stomach Mucosa	stomach
41	chr4:55453600-55453800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr4:55453600-55456800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:55453800-55454800	Weak transcription	Placenta	Placenta
44	chr4:55453800-55455000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr4:55454000-55455000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr4:55454400-55454600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr4:55454400-55455000	Enhancers	Fetal Heart	heart
48	chr4:55454400-55455200	Enhancers	Stomach Mucosa	stomach
49	chr4:55454600-55455200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr4:55454800-55455000	Enhancers	Placenta	Placenta

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